Canonical Allele Identifier: CA2066828477

Gene: HSPB8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119187117G= , CM000674.2:g.119187117G=	GRCh38
NC_000012.11:g.119624922G= , CM000674.1:g.119624922G=	GRCh37
NC_000012.10:g.118109305G=	NCBI36
NG_007953.2:g.13328G= , LRG_249:g.13328G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281938.7:c.431+29G= MANE Select	ENSP00000281938.3:n.431+29G=
ENST00000674542.1:c.368-6582G=	ENSP00000502352.1:n.368-6582G=
ENST00000674715.1:n.604+29G=
ENST00000674763.1:c.64+29G=
ENST00000674852.1:c.64+29G=
ENST00000675110.1:c.64+29G=
ENST00000675211.1:c.64+29G=
ENST00000675573.1:c.64+29G=
ENST00000675900.1:n.21+5081G=
ENST00000676071.1:n.164+29G=
ENST00000676244.1:n.137+29G=
ENST00000281938.6:c.431+29G=	ENSP00000281938.2:n.431+29G=
ENST00000541798.1:c.154+29G=
ENST00000542496.1:n.289+29G=
NM_014365.2:c.431+29G= , LRG_249t1:c.431+29G=	NP_055180.1:n.431+29G=
NM_014365.3:c.431+29G= MANE Select	NP_055180.1:n.431+29G=